NDC 71839-122 – Pantoprazole sodium

Pantoprazole Sodium 40 mg/10mL · Injection, Powder, For Solution · Intravenous

Human Prescription Drug 1 recall

Product NDC71839-122

Product details

Brand name
Pantoprazole sodium
Generic name
Pantoprazole sodium
Labeler
BE Pharmaceuticals Inc.
Dosage form
Injection, Powder, For Solution
Route
Intravenous
Marketing category
ANDA · ANDA216171
Marketed since
May 25, 2022
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Pantoprazole Sodium →

Package NDC codes (3)

Package NDCDescriptionSince
71839-122-011 VIAL in 1 CARTON (71839-122-01) / 10 mL in 1 VIALMay 25, 2022
71839-122-1010 CARTON in 1 PACKAGE (71839-122-10) / 1 VIAL in 1 CARTON / 10 mL in 1 VIALMay 25, 2022
71839-122-2525 CARTON in 1 PACKAGE (71839-122-25) / 1 VIAL in 1 CARTON / 10 mL in 1 VIALMay 25, 2022

Recalls mentioning this NDC

Other Pantoprazole Sodium products